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Hydrogen Bromide → Ethanone, 2,2-dibromo-1-(3-pyridinyl)-, hydrobromide

HRID 480399
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반응식

HRID 480399 반응식
C(OC(=O)[CH2:5][C:6]([C:8]1[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=1)=[O:7])C.[BrH:15].[Br:16]Br>>[BrH:15].[Br:15][CH:5]([Br:16])[C:6]([C:8]1[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=1)=[O:7]
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참가 물질

4

반응물 3

HCID 260Hydrogen BromideHCID 24408Bromine2회HCID 222197Ethyl 3-oxo-3-(pyridin-3-yl)propanoate

생성물 1

HCID 11984074Ethanone, 2,2-dibromo-1-(3-pyridinyl)-, hydrobromide수율 101.6%

실험 절차

3-(3-Pyridyl)-3-oxopropionic acid ethyl ester (1.95 g, 10.2 mmol) was added dropwise to 47% aqueous HBr solution (3.86 g) under ice-cooling. Bromine (2.2 g, 1.2 equivalent amount relative to 3-(3-pyridyl)-3-oxopropionic acid ethyl ester) was added dropwise at not more than 10° C. After stirring for 30 min, iced-water bath was removed and water (2 ml) and 47% aqueous HBr solution (4 ml) were added. The mixture was stirred at room temperature for 30 min. Furthermore, bromine (2.2 g, 1.2 equivalent amount relative to 3-(3-pyridyl)-3-oxopropionic acid ethyl ester) was added dropwise and the mixture was stirred at 65-70° C. After cooling to room temperature, the reaction mixture was filtrated to give 3.73 g of the titled compound (yield 95.2%).

후처리

  1. temperaturecooling
  2. customiced-water bath was removed
  3. additionwater (2 ml) and 47% aqueous HBr solution (4 ml) were added
  4. stirringThe mixture was stirred at room temperature for 30 min
  5. stirringthe mixture was stirred at 65-70° C
  6. filtrationthe reaction mixture was filtrated

출처 및 근거

ORD 기록
ord-0449178264dd4156835583e30d11d1b4
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06649768B1

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